Circulation. 2000;101:e188-e190
(Circulation. 2000;101:e188.)
© 2000 American Heart Association, Inc.
Circulation Electronic Pages |
Stentocarditis
Benno J. Rensing, MD;
Robert Jan van Geuns, MD;
Maarten Janssen, MD;
Matthijs Oudkerk, MD;
Pim J. de Feyter, MD
From the Department of Cardiology (B.J.R., R.J.v.G., M.J., P.J.d.F.),
Thoraxcenter, and Department of Radiology (M.O.), Dr Daniel den Hoed Kliniek,
Rotterdam, Netherlands.
Correspondence to Benno J. Rensing, MD, Thoraxcenter, BD 416, Dr Molewaterplein 40, 3015 GD Rotterdam, Netherlands. E-mail rensing{at}card.azr.nl
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Introduction
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Top
Introduction
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The patient was a
67-year-old man who had received 3 single
venous aortocoronary
bypass grafts in 1978. He remained free
of symptoms until mid-1998,
when he was admitted with unstable
angina. Angiography revealed severe
stenoses in the vein grafts
to both the right coronary
artery (RCA) and the obtuse marginal
(OM) branch of the circumflex
artery. Three stents were successfully
implanted in the OM graft, and 1
stent was implanted in the
graft to the RCA. The postprocedural course
was uneventful,
and the patient was discharged the next day. Four days
later,
however, he was readmitted with high fever, chills, and malaise.
Blood
cultures were repeatedly positive for
Staphylococcus
aureus,
and treatment with intravenous antibiotics was
begun. During
admission, he developed chest pain, with minimal
ST-segment
depression in the inferolateral ECG leads. Creatine
phosphokinase
levels rose to 1500 IU/L (normal <240 IU/L). An
extensive
search for the source of the infection was negative. We
decided
to perform an electron-beam tomographic (EBT, or ultrafast CT)
examination
of the thorax to look for a pulmonary, mediastinal,
or cardiac
source for the infection and to check bypass graft
patency.
Forty ECG-triggered, contrast-enhanced, consecutive tomograms were made
at inspiration, starting just above the aortic arch. Tomogram thickness
was set at 3 mm, with a 2-mm table increment after each
scan. Acquisition time was 100 ms. Contrast (150 mL) was injected at 4
mL/s through an arm vein. 3D volume renderings were made with Voxel
View software on a Silicon Graphics workstation.
The graft to the OM branch was found to be occluded (Figure 1
). Anterolateral to the ascending aorta,
a large mass was visible (Figure 2
). The
first and second stents of the OM graft were visible within the mass
(Figure 2
). Late contrast enhancement of the wall of the mass
was shown with an extra set of 15 tomograms over the upper anterior
mediastinum 2 minutes after contrast injection (Figure 2
). This
is very suggestive of an abscess.

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Figure 1. Volume rendering of basal part of heart and great
vessels. Patent single vein graft to left anterior descending
coronary artery (LAD) and its course over pulmonary
artery is indicated. Three radiopaque stents in occluded vein graft to
OM branch are indicated. Graft occlusion can be deduced by lack of
contrast material visible between stents.
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Figure 2. Single EBT tomograms at level of upper anterior
mediastinum acquired 2 minutes after contrast injection. Left, Lateral
and anterior to ascending aorta (Ao), a mass is visualized (asterisk).
Wall of mass is contrast-enhanced. This is very suggestive of an
abscess. Dense structure traversing mass from medial-anterior to
lateral-posterior are stent struts of first stent in occluded vein
graft. Right, Tomogram acquired 2 levels lower. At arrow, both first
and second stents are visible within abscess.
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The patient responded favorably to the medical treatment. Infection
parameters normalized, and after 6 weeks of treatment with
intravenous antibiotics, he could be discharged. A repeat
EBT investigation 4 months later showed complete disappearance of the
abscess (Figure 3
). The graft to the OM
branch remained occluded.

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Figure 3. Single EBT tomogram acquired 4 months later at
same level as Figure 2 , left. Mass has completely
disappeared.
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Footnotes
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The editor of Images in Cardiovascular Medicine is Hugh A. McAllister,
Jr, MD, Chief, Department of Pathology, St Lukes Episcopal
Hospital and Texas Heart Institute, and Clinical Professor of
Pathology, University of Texas Medical School and Baylor College
of Medicine.
Circulation encourages readers to submit cardiovascular images to Dr Hugh A. McAllister, Jr, St Lukes Episcopal Hospital and Texas Heart Institute, 6720 Bertner Ave, MC1-267, Houston, TX 77030.
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